Evidence map›Paper›PMID 26927799›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2016

HIV Skews the Lineage-Defining Transcriptional Profile of Mycobacterium tuberculosis-Specific CD4+ T Cells.

Catherine Riou, Natalie Strickland, Andreia P Soares, Björn Corleis, Douglas S Kwon, E John Wherry, Robert J Wilkinson, Wendy A Burgers

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.3field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Stages of pregnancy and HIV affect diagnosis of tuberculosis infection and Mycobacterium tuberculosis (MTB)-induced immune response: Findings from PRACHITi, a cohort study in Pune, India.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2021
    Article
  4. Th22 Cells Are a Major Contributor to the Mycobacterial CD4Journal of immunology (Baltimore, Md. : 1950) · 2021
    Article
  5. Article
  6. Article
  7. CD4 T Cells inFrontiers in immunology · 2020
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. CD4Trends in molecular medicine · 2017
    Review
  14. Characterization ofJournal of immunology (Baltimore, Md. : 1950) · 2017
    Article
  15. Analysis of the Phenotype ofFrontiers in immunology · 2017
    Article
  16. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 3 countries.

Catherine RiouDivision of Medical Virology, Department of Pathology, Faculty of Health Sciences, University of Cape Town, 7925, Cape Town, South Africa; Institute of Infectious Disease and Molecular Medicine, University of Cape Town, 7925, Cape Town, South Africa; c.riou@uct.ac.za.
Natalie StricklandDivision of Medical Virology, Department of Pathology, Faculty of Health Sciences, University of Cape Town, 7925, Cape Town, South Africa; Institute of Infectious Disease and Molecular Medicine, University of Cape Town, 7925, Cape Town, South Africa;
Andreia P SoaresDivision of Medical Virology, Department of Pathology, Faculty of Health Sciences, University of Cape Town, 7925, Cape Town, South Africa; Institute of Infectious Disease and Molecular Medicine, University of Cape Town, 7925, Cape Town, South Africa;ORCID http://orcid.org/0000-0002-9003-222X
Björn CorleisRagon Institute of MGH, MIT and Harvard, Cambridge, MA 02139; Division of Infectious Diseases, Massachusetts General Hospital, Boston, MA 02139;ORCID http://orcid.org/0000-0001-9833-3169
Douglas S KwonRagon Institute of MGH, MIT and Harvard, Cambridge, MA 02139; Division of Infectious Diseases, Massachusetts General Hospital, Boston, MA 02139;ORCID http://orcid.org/0000-0001-8521-8735
E John WherryDepartment of Microbiology, Institute for Immunology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104;
Robert J WilkinsonInstitute of Infectious Disease and Molecular Medicine, University of Cape Town, 7925, Cape Town, South Africa; Department of Medicine, Imperial College London, London W21 PG, United Kingdom; Francis Crick Institute Mill Hill Laboratory, London NW7 1AA, United Kingdom; and Clinical Infectious Diseases Research Initiative, University of Cape Town, 7925, Cape Town, South Africa.ORCID http://orcid.org/0000-0002-2753-1800
Wendy A BurgersDivision of Medical Virology, Department of Pathology, Faculty of Health Sciences, University of Cape Town, 7925, Cape Town, South Africa; Institute of Infectious Disease and Molecular Medicine, University of Cape Town, 7925, Cape Town, South Africa;
University of Cape Town · ZARagon Institute of MGH, MIT and Harvard · USUniversity of Pennsylvania · US

Funding

Virus & Reservoirs CoreP30AI045008 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI ROBERT GROSS · 1999 to 2026
$78.6M
Inflammatory determinants of disease severity and treatment outcome in TB patientsU01AI115940 · NIAID · UNIVERSITY OF CAPE TOWN · PI SHER, ALAN, WILKINSON, ROBERT JOHN · 2015 to 2019
$1.1M
Diversity of CD4+ Th subsets in TB immunity - Impact of HIV infectionR21AI115977 · NIAID · UNIVERSITY OF CAPE TOWN · PI RIOU, CATHERINE, WHERRY, E. JOHN · 2015 to 2016
$351k
Medical Research Council MC_U117588499Medical Research Council U1175.02.002.00014.01NIAID NIH HHS P30 AI045008NIAID NIH HHS R21 AI115977NIAID NIH HHS R21AI115977NIAID NIH HHS U01 AI115940Wellcome Trust 089832Wellcome Trust 089832/Z/09/ZWellcome Trust 104803
6 · The paper itself

Abstract

HIV-infected persons are at greater risk of developing tuberculosis (TB) even before profound CD4 loss occurs, suggesting that HIV alters CD4(+) T cell functions capable of containing bacterial replication. An effective immune response to Mycobacterium tuberculosis most likely relies on the development of a balanced CD4 response, in which distinct CD4(+) Th subsets act in synergy to control the infection. To define the diversity of M. tuberculosis-specific CD4(+) Th subsets and determine whether HIV infection impacts such responses, the expression of lineage-defining transcription factors T-bet, Gata3, RORγt, and Foxp3 was measured in M. tuberculosis-specific CD4(+) T cells in HIV-uninfected (n = 20) and HIV-infected individuals (n = 20) with latent TB infection. Our results show that, upon 5-d restimulation in vitro, M. tuberculosis-specific CD4(+) T cells from healthy individuals have the ability to exhibit a broad spectrum of Th subsets, defined by specific patterns of transcription factor coexpression. These transcription factor profiles were skewed in HIV-infected individuals where the proportion of T-bet(high)Foxp3(+) M. tuberculosis-specific CD4(+) T cells was significantly decreased (p = 0.002) compared with HIV-uninfected individuals, a change that correlated inversely with HIV viral load (p = 0.0007) and plasma TNF-α (p = 0.027). Our data demonstrate an important balance in Th subset diversity defined by lineage-defining transcription factor coexpression profiles that is disrupted by HIV infection and suggest a role for HIV in impairing TB immunity by altering the equilibrium of M. tuberculosis-specific CD4(+) Th subsets.

Indexed as

TranscriptomeAdultCase-Control StudiesCD4 Lymphocyte CountCD4-Positive T-LymphocytesCell LineageCoinfectionCytokinesFemaleGene ExpressionHIV InfectionsHumansLymphocyte ActivationMaleMycobacterium tuberculosisTime FactorsCytokinesTranscription FactorsTuberculin

Identifiers

PMID26927799
PMCPMC4799776
OpenAlexW2288310659

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.